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  2. Pharmacovigilance - Wikipedia

    en.wikipedia.org/wiki/Pharmacovigilance

    The CIOMS, a part of the WHO, is globally oriented think tank that provides guidance on drug safety related topics through its Working Groups. [citation needed] The CIOMS prepares reports that are used as a reference for developing future drug regulatory policy and procedures, and over the years, many of CIOMS' proposed policies have been adopted.

  3. FDA Adverse Event Reporting System - Wikipedia

    en.wikipedia.org/wiki/FDA_Adverse_Event...

    Based on an evaluation of the potential safety concern, The FDA may take regulatory action(s) to improve product safety and protect the public health, such as updating a product's labeling information, restricting the use of the drug, communicating new safety information to the public, or, in rare cases, removing a product from the market.

  4. Research on Adverse Drug Events and Reports - Wikipedia

    en.wikipedia.org/wiki/Research_on_Adverse_Drug...

    The aims of RADAR are to disseminate safety reports for serious adverse drug reactions (sADRs) and to identify barriers to identification and reporting of these clinical events. Investigators have developed a well-coordinated system to accurately compile case report information on sADRs and to identify milestones associated with identification ...

  5. Template:Infobox drug/doc/FDA-2023 - Wikipedia

    en.wikipedia.org/wiki/Template:Infobox_drug/doc/...

    Orange Book (Approved Drug Products with Therapeutic Equivalence Evaluations) Search 16. OMUF OTC Monographs@FDA 17. Outsourcing Facility Product Report. 18. Postmarket Requirements and Commitments Search 19. PEPFAR President's Emergency Plan for AIDS Relief (PEPFAR) Database 20. Product-Specific Guidances for Generic Drug Development Database 21.

  6. VigiBase - Wikipedia

    en.wikipedia.org/wiki/VigiBase

    VigiBase is a World Health Organization's (WHO) global Individual Case Safety Report (ICSR) database that contains ICSRs submitted by the participating member states enrolled under WHO's international drug monitoring programme. It is the single largest drug safety data repository in the world.

  7. Qualified Person Responsible For Pharmacovigilance - Wikipedia

    en.wikipedia.org/wiki/Qualified_Person...

    The QPPV must reside in the EU, and should be permanently and continuously at the disposal of the MAH. Each company (i.e. Applicant/Marketing Authorisation Holder or group of Marketing Authorisation Holders using a common pharmacovigilance system) should appoint one QPPV responsible for overall pharmacovigilance for all medicinal products for which the company holds marketing authorisations ...

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  9. Template:Infobox drug/testcases-warning - Wikipedia

    en.wikipedia.org/wiki/Template:Infobox_drug/test...

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